Canonical Allele Identifier: CA545410432

Gene:

Linked Data

• dbSNP Id: rs1416716316
• gnomAD v2: 3-109462264-C-G
• gnomAD v3: 3-109743417-C-G
• gnomAD v4: 3-109743417-C-G
• MyVariant Identifiers: chr3:g.109462264C>G (hg19) ; chr3:g.109743417C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.109743417C>G , CM000665.2:g.109743417C>G	GRCh38
NC_000003.11:g.109462264C>G , CM000665.1:g.109462264C>G	GRCh37
NC_000003.10:g.110944954C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_924325.1:n.142+63222C>G